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Fungal Morphology, Iron Homeostasis, and Lipid Metabolism Regulated by a GATA Transcription Factor in Blastomyces dermatitidis

In response to temperature, Blastomyces dermatitidis converts between yeast and mold forms. Knowledge of the mechanism(s) underlying this response to temperature remains limited. In B. dermatitidis, we identified a GATA transcription factor, SREB, important for the transition to mold. Null mutants (...

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Autores principales: Marty, Amber J., Broman, Aimee T., Zarnowski, Robert, Dwyer, Teigan G., Bond, Laura M., Lounes-Hadj Sahraoui, Anissa, Fontaine, Joël, Ntambi, James M., Keleş, Sündüz, Kendziorski, Christina, Gauthier, Gregory M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482641/
https://www.ncbi.nlm.nih.gov/pubmed/26114571
http://dx.doi.org/10.1371/journal.ppat.1004959
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author Marty, Amber J.
Broman, Aimee T.
Zarnowski, Robert
Dwyer, Teigan G.
Bond, Laura M.
Lounes-Hadj Sahraoui, Anissa
Fontaine, Joël
Ntambi, James M.
Keleş, Sündüz
Kendziorski, Christina
Gauthier, Gregory M.
author_facet Marty, Amber J.
Broman, Aimee T.
Zarnowski, Robert
Dwyer, Teigan G.
Bond, Laura M.
Lounes-Hadj Sahraoui, Anissa
Fontaine, Joël
Ntambi, James M.
Keleş, Sündüz
Kendziorski, Christina
Gauthier, Gregory M.
author_sort Marty, Amber J.
collection PubMed
description In response to temperature, Blastomyces dermatitidis converts between yeast and mold forms. Knowledge of the mechanism(s) underlying this response to temperature remains limited. In B. dermatitidis, we identified a GATA transcription factor, SREB, important for the transition to mold. Null mutants (SREBΔ) fail to fully complete the conversion to mold and cannot properly regulate siderophore biosynthesis. To capture the transcriptional response regulated by SREB early in the phase transition (0–48 hours), gene expression microarrays were used to compare SREB∆ to an isogenic wild type isolate. Analysis of the time course microarray data demonstrated SREB functioned as a transcriptional regulator at 37°C and 22°C. Bioinformatic and biochemical analyses indicated SREB was involved in diverse biological processes including iron homeostasis, biosynthesis of triacylglycerol and ergosterol, and lipid droplet formation. Integration of microarray data, bioinformatics, and chromatin immunoprecipitation identified a subset of genes directly bound and regulated by SREB in vivo in yeast (37°C) and during the phase transition to mold (22°C). This included genes involved with siderophore biosynthesis and uptake, iron homeostasis, and genes unrelated to iron assimilation. Functional analysis suggested that lipid droplets were actively metabolized during the phase transition and lipid metabolism may contribute to filamentous growth at 22°C. Chromatin immunoprecipitation, RNA interference, and overexpression analyses suggested that SREB was in a negative regulatory circuit with the bZIP transcription factor encoded by HAPX. Both SREB and HAPX affected morphogenesis at 22°C; however, large changes in transcript abundance by gene deletion for SREB or strong overexpression for HAPX were required to alter the phase transition.
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spelling pubmed-44826412015-06-29 Fungal Morphology, Iron Homeostasis, and Lipid Metabolism Regulated by a GATA Transcription Factor in Blastomyces dermatitidis Marty, Amber J. Broman, Aimee T. Zarnowski, Robert Dwyer, Teigan G. Bond, Laura M. Lounes-Hadj Sahraoui, Anissa Fontaine, Joël Ntambi, James M. Keleş, Sündüz Kendziorski, Christina Gauthier, Gregory M. PLoS Pathog Research Article In response to temperature, Blastomyces dermatitidis converts between yeast and mold forms. Knowledge of the mechanism(s) underlying this response to temperature remains limited. In B. dermatitidis, we identified a GATA transcription factor, SREB, important for the transition to mold. Null mutants (SREBΔ) fail to fully complete the conversion to mold and cannot properly regulate siderophore biosynthesis. To capture the transcriptional response regulated by SREB early in the phase transition (0–48 hours), gene expression microarrays were used to compare SREB∆ to an isogenic wild type isolate. Analysis of the time course microarray data demonstrated SREB functioned as a transcriptional regulator at 37°C and 22°C. Bioinformatic and biochemical analyses indicated SREB was involved in diverse biological processes including iron homeostasis, biosynthesis of triacylglycerol and ergosterol, and lipid droplet formation. Integration of microarray data, bioinformatics, and chromatin immunoprecipitation identified a subset of genes directly bound and regulated by SREB in vivo in yeast (37°C) and during the phase transition to mold (22°C). This included genes involved with siderophore biosynthesis and uptake, iron homeostasis, and genes unrelated to iron assimilation. Functional analysis suggested that lipid droplets were actively metabolized during the phase transition and lipid metabolism may contribute to filamentous growth at 22°C. Chromatin immunoprecipitation, RNA interference, and overexpression analyses suggested that SREB was in a negative regulatory circuit with the bZIP transcription factor encoded by HAPX. Both SREB and HAPX affected morphogenesis at 22°C; however, large changes in transcript abundance by gene deletion for SREB or strong overexpression for HAPX were required to alter the phase transition. Public Library of Science 2015-06-26 /pmc/articles/PMC4482641/ /pubmed/26114571 http://dx.doi.org/10.1371/journal.ppat.1004959 Text en © 2015 Marty et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Marty, Amber J.
Broman, Aimee T.
Zarnowski, Robert
Dwyer, Teigan G.
Bond, Laura M.
Lounes-Hadj Sahraoui, Anissa
Fontaine, Joël
Ntambi, James M.
Keleş, Sündüz
Kendziorski, Christina
Gauthier, Gregory M.
Fungal Morphology, Iron Homeostasis, and Lipid Metabolism Regulated by a GATA Transcription Factor in Blastomyces dermatitidis
title Fungal Morphology, Iron Homeostasis, and Lipid Metabolism Regulated by a GATA Transcription Factor in Blastomyces dermatitidis
title_full Fungal Morphology, Iron Homeostasis, and Lipid Metabolism Regulated by a GATA Transcription Factor in Blastomyces dermatitidis
title_fullStr Fungal Morphology, Iron Homeostasis, and Lipid Metabolism Regulated by a GATA Transcription Factor in Blastomyces dermatitidis
title_full_unstemmed Fungal Morphology, Iron Homeostasis, and Lipid Metabolism Regulated by a GATA Transcription Factor in Blastomyces dermatitidis
title_short Fungal Morphology, Iron Homeostasis, and Lipid Metabolism Regulated by a GATA Transcription Factor in Blastomyces dermatitidis
title_sort fungal morphology, iron homeostasis, and lipid metabolism regulated by a gata transcription factor in blastomyces dermatitidis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482641/
https://www.ncbi.nlm.nih.gov/pubmed/26114571
http://dx.doi.org/10.1371/journal.ppat.1004959
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